Canonical Allele Identifier: CA409207828

Gene: SLC12A5

Linked Data

• dbSNP Id: rs1243967726
• gnomAD v3: 20-46056462-A-T
• gnomAD v4: 20-46056462-A-T
• MyVariant Identifiers: chr20:g.44685101A>T (hg19) ; chr20:g.46056462A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46056462A>T , CM000682.2:g.46056462A>T	GRCh38
NC_000020.10:g.44685101A>T , CM000682.1:g.44685101A>T	GRCh37
NC_000020.9:g.44118508A>T	NCBI36
NG_046341.1:g.39773A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243964.7:c.3008A>T MANE Select	ENSP00000243964.4:p.Lys1003Met
ENST00000243964.6:c.3008A>T	ENSP00000243964.3:p.Lys1003Met
ENST00000454036.6:c.3077A>T	ENSP00000387694.1:p.Lys1026Met
ENST00000616201.4:c.1298-2194A>T	ENSP00000484585.1:n.1298-2194A>T
ENST00000616202.4:c.613-2019A>T	ENSP00000478369.1:n.613-2019A>T
ENST00000616933.4:c.*2326A>T	ENSP00000477569.1:n.*2326A>T
ENST00000626937.2:c.510-3137A>T	ENSP00000485953.1:n.510-3137A>T
ENST00000628413.1:n.524A>T
NM_001134771.1:c.3077A>T	NP_001128243.1:p.Lys1026Met
NM_020708.4:c.3008A>T	NP_065759.1:p.Lys1003Met
XM_017027981.1:c.3077A>T	XP_016883470.1:p.Lys1026Met
NM_001134771.2:c.3077A>T	NP_001128243.1:p.Lys1026Met
NM_020708.5:c.3008A>T MANE Select	NP_065759.1:p.Lys1003Met